Shih Ruey-Horng, Wang Chen-Yu, Yang Chuen-Mao
Institute of Neuroscience, National Chengchi University Taipei, Taiwan.
Department of Physiology and Pharmacology and Health Aging Research Center, College of Medicine, Chang Gung University Tao-Yuan, Taiwan.
Front Mol Neurosci. 2015 Dec 18;8:77. doi: 10.3389/fnmol.2015.00077. eCollection 2015.
The NF-κB (nuclear factor κ-light-chain-enhancer of activated B cells) transcription factor family is a pleiotropic regulator of many cellular signaling pathways, providing a mechanism for the cells in response to a wide variety of stimuli linking to inflammation. The stimulated cells will be regulated by not only the canonical but also non-canonical NF-κB pathways. To initiate both of these pathways, IκB-degradation triggers NF-κB release and the nuclear translocated-heterodimer (or homodimer) can associate with the κB sites of promoter to regulate the gene transcriptions. NF-κB ubiquitously expresses in neurons and the constitutive NF-κB activation is associated with processing of neuronal information. NF-κB can regulate the transcription of genes such as chemokines, cytokines, proinflammatory enzymes, adhesion molecules, proinflammatory transcription factors, and other factors to modulate the neuronal survival. In neuronal insult, NF-κB constitutively active in neuron cell bodies can protect neurons against different injuries and regulate the neuronal inflammatory reactions. Besides neurons, NF-κB transcription factors are abundant in glial cells and cerebral blood vessels and the diverse functions of NF-κB also regulate the inflammatory reaction around the neuronal environment. NF-κB transcription factors are abundant in the brain and exhibit diverse functions. Several central nerve system (CNS) diseases are linked to NF-κB activated by inflammatory mediators. The RelA and c-Rel expression produce opposite effects on neuronal survival. Importantly, c-Rel expression in CNS plays a critical role in anti-apoptosis and reduces the age-related behaviors. Moreover, the different subunits of NF-κB dimer formation can modulate the neuroninflammation, neuronal protection, or neurotoxicity. The diverse functions of NF-κB depend on the subunits of the NF-κB dimer-formation which enable us to develop a therapeutic approach to neuroinflammation based on a new concept of inflammation as a strategic tool in neuronal cells. However, the detail role of NF-κB in neuroinflammation, remains to be clarified. In the present article, we provide an updated review of the current state of our knowledge about relationship between NF-κB and neuroinflammation.
核因子κB(NF-κB,即活化B细胞核因子κ轻链增强子)转录因子家族是多种细胞信号通路的多效性调节因子,为细胞提供了一种机制,以响应与炎症相关的多种刺激。受刺激的细胞不仅会受到经典NF-κB通路的调控,还会受到非经典NF-κB通路的调控。为启动这两条通路,IκB降解会触发NF-κB释放,核转位的异源二聚体(或同源二聚体)可与启动子的κB位点结合,从而调控基因转录。NF-κB在神经元中普遍表达,其组成型激活与神经元信息处理有关。NF-κB可调节趋化因子、细胞因子、促炎酶、黏附分子、促炎转录因子等基因的转录,从而调节神经元存活。在神经元损伤时,神经元细胞体中组成型激活的NF-κB可保护神经元免受不同损伤,并调节神经元炎症反应。除神经元外,NF-κB转录因子在胶质细胞和脑血管中也很丰富,NF-κB的多种功能也调节着神经元周围环境的炎症反应。NF-κB转录因子在大脑中丰富,并具有多种功能。几种中枢神经系统(CNS)疾病与炎症介质激活的NF-κB有关。RelA和c-Rel的表达对神经元存活产生相反的影响。重要的是,CNS中的c-Rel表达在抗凋亡中起关键作用,并减少与年龄相关的行为。此外,NF-κB二聚体形成的不同亚基可调节神经元炎症、神经元保护或神经毒性。NF-κB的多种功能取决于NF-κB二聚体形成的亚基,这使我们能够基于炎症作为神经元细胞中的一种战略工具这一新概念,开发一种针对神经炎症的治疗方法。然而,NF-κB在神经炎症中的具体作用仍有待阐明。在本文中,我们提供了关于NF-κB与神经炎症之间关系的当前知识状态的最新综述。